ClinVar Miner

Submissions for variant NM_006912.6(RIT1):c.163+12C>A

gnomAD frequency: 0.00001  dbSNP: rs372092063
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002219071 SCV002378154 likely benign Noonan syndrome 8 2024-09-30 criteria provided, single submitter clinical testing

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